FDA.reportPublic FDA data

DURADRY AM

Manufacturer
Novadore USA, LLC
Effective date
2021-06-07
Label type
HUMAN OTC DRUG LABEL
Version
8
Source
full-release
Hydrated at
2026-05-31 23:40:45

Label at a glance#

ProductDURADRY AM
Active ingredientALUMINUM ZIRCONIUM TRICHLOROHYDREX GLY
Label structure11 sections

Indications and uses

Reduces underarm perspiration

Dosage and administration

Apply to underarms only.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Aluminum Zirconium Trichlorohydrex Glycine 20%

Purpose

OTC - PURPOSE SECTION

Antiperspirant

Uses

INDICATIONS & USAGE SECTION

Reduces underarm perspiration

Warnings

WARNINGS SECTION

For external use only
Stop use if rash or irritation occurs.

Do not use

OTC - DO NOT USE SECTION

  • On broken skin.

Ask a doctor before use

OTC - ASK DOCTOR SECTION

if you have kidney disease

Keep out of reach of children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

  • Apply to underarms only.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Cyclopentasiloxane, Stearyl Alcohol, PPG-14 Butyl Ether, C12-15 Alkyl Benzoate, Hydrogenated Castor Oil, Dimethicone, Zinc Ricinoleate, Petrolatum, Aluminum Starch Octenylsuccinate Fragrance.

Questions?

OTC - QUESTIONS SECTION

Visit us at www.duradry.com/am

Designed & developed by:
NOVADORE USA, INC
Miami, FL

DURADRY AM (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYCINE)

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Duradry AMDuradry AM

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
69990-200-012023-01-30C16284748780-1f386c649-b01a-0266-e053-dadaa90a7c1aDURADRY AM Antiperspirant/Deodorant for everyday use

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
69990-200-01DURADRY AM65 g in 1 CYLINDERSTICK658
69990-200-01DURADRY AM1 in 1 CARTONSTICK18

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
69990-200DURADRY AM (ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYCINE) STICK [NOVADORE USA, LLC]8Legacy NDC, 2 package rows20210608_d5f5ce95-6e5a-48fc-949a-c2986d8f7515.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 12 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
69990-20069990-200-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 10 matching rows.

Name, UNII, Kind table
NameUNIIKind
CYCLOMETHICONE 50THT5PCI0RIACT
STEARYL ALCOHOL2KR89I4H1YIACT
PPG-14 BUTYL ETHERR199TJT95TIACT
ALKYL (C12-15) BENZOATEA9EJ3J61HQIACT
HYDROGENATED CASTOR OILZF94AP8MEYIACT
DIMETHICONE92RU3N3Y1OIACT
ZINC RICINOLEATEBOH1Z111J2IACT
PETROLATUM4T6H12BN9UIACT
ALUMINUM STARCH OCTENYLSUCCINATEI9PJ0O6294IACT
ALUMINUM ZIRCONIUM TRICHLOROHYDREX GLYT27D6T99LHACTIB

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
c4338188-703f-06ba-e053-2995a90a1969d5f5ce95-6e5a-48fc-949a-c2986d8f75152021-06-07WarningsExact identifier
spl id: c4338188-703f-06ba-e053-2995a90a1969
spl set id: d5f5ce95-6e5a-48fc-949a-c2986d8f7515

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.